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. 2009 Sep 11;4(9):e6965. doi: 10.1371/journal.pone.0006965

Table 2. Predicted epitopes based on the HLA-B7 supertype motif and the clade A1 OLP library sequence used for epitope mapping.

U15119 position Seqence TAP binding scores* ITOPIA HLA-B*0702 binding (%)** Autologous Seq.***
8–16 YPCWWTWGI 2.893 none no data
75–83 DPNPQEIYM −0.901 none DPNPQEIELDPNPREISLDPNPQEIPLDPNPQEVVL
114–22 KPCVQLTPL 2.175 64.2(----K----) KPCVKLTPL KPCVQLTPLKPCVKLTPLKPCVKLTPL
205–13 CPKVTFEPI −1.025 30.1 CPKVNFEPICPKVTFEPICPKVSFEPICPKVTFEPI
211–9 EPIPIRYCA 2.869 none EPIPIHYCAEPIPIHYCAEPIPIHYCAEPIPIHYCA
213–21 IPIRYCAPA 0.198 58.5(---H-----) IPIHYCAPAIPIHYCAPAIPIHYCAPAIPIHYCAPA
252–60 RPVVSTQLL 1.393 78.1 KPVVSTQLLKPVVSTQLLKPVVSTQLLKPVVSTQLL
408–16 LPCRIKQII 2.046 75.9 no data
489–497 APTKAKRRV 2.482 95.2 no data
843–51 IPRRIRQGL 3.59 (intermed) 180.2 no data

Only the last epitope (in bold) was recognized.

*

TAP binding scores were calculated using TAPpred, as per Ref. 20.

**

Percentage of Positive control binding. Where ITOPIA-tested sequences differed from OLP, these are noted.

***

Autologous sequences are from HLA B7 supertype+ subjects who did not recognize the epitopes listed (except IPRRIRQGL). Each sequence = 1 subject.